File:Barnes Figure.png
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Most cases of pentosan polysulfate maculopathy that involve the peripapillary retina, demonstrate a hypoautofluorescent peripapillary ring (A). The autofluorescent signal is spared in many inherited macular dystrophies such as this dominant macular dystrophy associated with a variant of unknown significance in the ELOVL4 gene (B), another macular dystrophy associated with a disease-causing PRPH2 variant (C), and two disease-causing ABCA4 variants (D). Reprinted with permission from Elsevier from: Barnes AC, Hanif AM, Jain N. Pentosan polysulfate maculopathy versus inherited macular dystrophies: comparative assessment with multimodal imaging. Ophthalmol Retina. Published online May 21, 2020. doi:10.1016/j.oret.2020.05.008
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 13:08, January 22, 2021 | | 918 × 665 (739 KB) | Nieraj.Jain (talk | contribs) | Most cases of pentosan polysulfate maculopathy that involve the peripapillary retina, demonstrate a hypoautofluorescent peripapillary ring (A). The autofluorescent signal is spared in many inherited macular dystrophies such as this dominant macular dys... |
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